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FI843643A0 - 2,5-disubstituerade-4(3h)-pyrimidoner med histamin-h2-receptor antagonistaktivitet. - Google Patents

2,5-disubstituerade-4(3h)-pyrimidoner med histamin-h2-receptor antagonistaktivitet.

Info

Publication number
FI843643A0
FI843643A0 FI843643A FI843643A FI843643A0 FI 843643 A0 FI843643 A0 FI 843643A0 FI 843643 A FI843643 A FI 843643A FI 843643 A FI843643 A FI 843643A FI 843643 A0 FI843643 A0 FI 843643A0
Authority
FI
Finland
Prior art keywords
pyrimidoner
disubstituerade
antagonistactivity
histamine
receptor
Prior art date
Application number
FI843643A
Other languages
English (en)
Other versions
FI83868C (fi
FI843643L (fi
FI83868B (fi
Inventor
Aldo A Algieri
Original Assignee
Bristol Myers Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bristol Myers Co filed Critical Bristol Myers Co
Publication of FI843643A0 publication Critical patent/FI843643A0/fi
Publication of FI843643L publication Critical patent/FI843643L/fi
Application granted granted Critical
Publication of FI83868B publication Critical patent/FI83868B/fi
Publication of FI83868C publication Critical patent/FI83868C/fi

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/32One oxygen, sulfur or nitrogen atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/47One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/48Two nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/08Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
    • C07D295/096Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
FI843643A 1983-09-21 1984-09-18 Foerfarande foer framstaellning av terapeutiskt aktiva 2,5-disubstituerade 4(3h)-pyrimidoner. FI83868C (fi)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US53442683 1983-09-21
US06/534,426 US4772704A (en) 1983-09-21 1983-09-21 2,5-disubstituted-4(3H)-pyrimidones having histamine H2 -receptor antagonist activity

Publications (4)

Publication Number Publication Date
FI843643A0 true FI843643A0 (fi) 1984-09-18
FI843643L FI843643L (fi) 1985-03-22
FI83868B FI83868B (fi) 1991-05-31
FI83868C FI83868C (fi) 1991-09-10

Family

ID=24129972

Family Applications (1)

Application Number Title Priority Date Filing Date
FI843643A FI83868C (fi) 1983-09-21 1984-09-18 Foerfarande foer framstaellning av terapeutiskt aktiva 2,5-disubstituerade 4(3h)-pyrimidoner.

Country Status (36)

Country Link
US (1) US4772704A (fi)
JP (1) JPH0643310B2 (fi)
KR (1) KR900001198B1 (fi)
AR (2) AR242385A1 (fi)
AT (1) AT387965B (fi)
AU (1) AU583479B2 (fi)
BE (1) BE900652A (fi)
CA (1) CA1260463A (fi)
CH (1) CH665840A5 (fi)
CS (1) CS249147B2 (fi)
CY (1) CY1561A (fi)
DD (1) DD226881A5 (fi)
DE (1) DE3434578A1 (fi)
DK (1) DK162987C (fi)
ES (4) ES8607253A1 (fi)
FI (1) FI83868C (fi)
FR (1) FR2552082B1 (fi)
GB (1) GB2146994B (fi)
GR (1) GR80439B (fi)
HK (1) HK73790A (fi)
HU (1) HU193227B (fi)
IE (1) IE58083B1 (fi)
IL (1) IL72990A (fi)
IT (1) IT1176739B (fi)
LU (1) LU85550A1 (fi)
NL (1) NL8402898A (fi)
NO (1) NO161561C (fi)
NZ (1) NZ209572A (fi)
OA (1) OA07820A (fi)
PT (1) PT79256B (fi)
SE (1) SE463209B (fi)
SG (1) SG60890G (fi)
YU (1) YU45205B (fi)
ZA (1) ZA847345B (fi)
ZM (1) ZM4984A1 (fi)
ZW (1) ZW16084A1 (fi)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2873340B2 (ja) * 1988-04-29 1999-03-24 武田薬品工業株式会社 抗生物質tan―1057,その製造法および用途
US20230349922A1 (en) 2020-08-11 2023-11-02 Université De Strasbourg H2 Blockers Targeting Liver Macrophages for the Prevention and Treatment of Liver Disease and Cancer

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IN151188B (fi) * 1978-02-13 1983-03-05 Smith Kline French Lab
ES477520A1 (es) * 1978-02-25 1979-06-01 Thomae Gmbh Dr K Procedimiento para la preparacion de nuevas penicilinas.
IL57005A (en) * 1978-04-11 1983-11-30 Smith Kline French Lab Process for the preparation of 2-amino pyrimid-4-one derivatives and novel 2-nitroaminopyrimid-4-ones as intermediates therefor
US4496567A (en) * 1978-11-13 1985-01-29 Smith Kline & French Laboratories Limited Phenyl alkylaminopyrimidones
US4521418A (en) * 1979-02-21 1985-06-04 Smith Kline & French Laboratories Limited Guanidinothiazolyl derivatives
AU531142B2 (en) * 1979-04-04 1983-08-11 Smith Kline & French Laboratories Limited 2 amino- pyimindones
CA1140129A (en) * 1979-08-21 1983-01-25 Ronald J. King 4-pyrimidone derivatives
ZW21281A1 (en) * 1980-10-01 1981-11-18 Smith Kline French Lab Amine derivatives
US4352933A (en) * 1981-02-06 1982-10-05 Smithkline Beckman Corporation Chemical methods and intermediates for preparing substituted pyrimidinones
NZ202797A (en) * 1981-12-28 1985-08-30 Lilly Co Eli Pyrimidine derivatives and pharmaceutical compositions
US4468399A (en) * 1981-12-28 1984-08-28 Eli Lilly And Company 2-[2-(2-Aminoalkyl-4-thiazolylmethylthio)alkyl]-amino-5-substituted-4-pyrimidones
GB8320505D0 (en) * 1983-07-29 1983-09-01 Smith Kline French Lab Chemical compounds
CA1275097A (en) * 1984-10-02 1990-10-09 Fujio Nohara Pyridyloxy derivatives

Also Published As

Publication number Publication date
DK450484D0 (da) 1984-09-20
KR900001198B1 (ko) 1990-02-28
PT79256A (en) 1984-10-01
OA07820A (fr) 1986-11-20
IT8422744A0 (it) 1984-09-20
ES8607253A1 (es) 1986-05-16
YU45205B (en) 1992-05-28
ZM4984A1 (en) 1985-05-21
AT387965B (de) 1989-04-10
FR2552082B1 (fr) 1987-02-20
SG60890G (en) 1990-09-07
GR80439B (en) 1985-01-22
SE8404729D0 (sv) 1984-09-20
ZW16084A1 (en) 1985-01-16
FR2552082A1 (fr) 1985-03-22
SE463209B (sv) 1990-10-22
IT1176739B (it) 1987-08-18
ES544213A0 (es) 1987-04-01
NO843726L (no) 1985-03-22
GB2146994B (en) 1987-09-03
YU161384A (en) 1987-12-31
SE8404729L (sv) 1985-03-22
GB8423863D0 (en) 1984-10-24
AU583479B2 (en) 1989-05-04
AU3335184A (en) 1985-03-28
KR850002259A (ko) 1985-05-10
BE900652A (fr) 1985-03-21
GB2146994A (en) 1985-05-01
FI83868C (fi) 1991-09-10
CH665840A5 (de) 1988-06-15
NL8402898A (nl) 1985-04-16
AR242385A1 (es) 1993-03-31
ES551501A0 (es) 1987-01-16
HUT35259A (en) 1985-06-28
ES8704465A1 (es) 1987-04-01
ES551500A0 (es) 1987-03-16
DK162987C (da) 1992-06-01
LU85550A1 (fr) 1985-06-04
ES536054A0 (es) 1986-05-16
AR242789A1 (es) 1993-05-31
FI843643L (fi) 1985-03-22
HK73790A (en) 1990-09-28
ES8704155A1 (es) 1987-03-16
US4772704A (en) 1988-09-20
CY1561A (en) 1991-03-22
NZ209572A (en) 1988-05-30
DK450484A (da) 1985-03-22
IE842406L (en) 1985-03-21
FI83868B (fi) 1991-05-31
ZA847345B (en) 1985-06-26
NO161561B (no) 1989-05-22
IE58083B1 (en) 1993-06-30
HU193227B (en) 1987-08-28
DK162987B (da) 1992-01-06
NO161561C (no) 1989-08-30
JPH0643310B2 (ja) 1994-06-08
JPS6087271A (ja) 1985-05-16
IL72990A (en) 1990-07-12
CS249147B2 (en) 1987-03-12
ATA300984A (de) 1988-09-15
ES8702897A1 (es) 1987-01-16
CA1260463A (en) 1989-09-26
IT8422744A1 (it) 1986-03-20
PT79256B (en) 1986-11-20
DD226881A5 (de) 1985-09-04
DE3434578A1 (de) 1985-04-11

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Legal Events

Date Code Title Description
MM Patent lapsed
MM Patent lapsed

Owner name: BRISTOL-MYERS SQUIBB COMPANY